Cosmetic or pharmeceutical composition containing a black horehound extract

ABSTRACT

A black horehound extract is used to prepare a cosmetic or pharmaceutical composition, particularly a dermatological composition, for promoting skin pigmentation, preventing or delaying the growth of grey hairs, treating pigmentary disorders, reducing triglyceride levels in fat cells, and preventing the build-up of body fat such as in cellulite. The composition may particularly be used effectively to promote skin or hair pigmentation and a reduction in the build-up of body fat such as in cellulite.

This is a divisional of application Ser. No. 08/244,582, filed as PCT/FR92/01105, Nov. 27, 1992, now U.S. Pat. No. 5,514,374.

The present invention relates essentially to a cosmetic or pharmaceutical composition, especially dermatological composition, containing an extract of black borehound, intended in particular for promoting the pigmentation of the skin or hair or for reducing the amount of triglycerides in the adipocytes, and to the process for its manufacture.

The present invention further relates to the use of an extract of black borehound for the preparation of such a cosmetic or pharmaceutical composition intended in particular for treating pigmentation disorders or for reducing the amount of triglycerides in the adipocytes.

The plants of the genus Ballota belong to the family of the Labiatae, which are found in temperate regions. An example which may be mentioned is Ballota nigra (LINN.) or Ballota foetida, also known as black borehound. This is a common perennial plant which is found particularly in uncultivated places, along hedges, paths or walls. It has a most unpleasant smell. Other examples which may be mentioned are Ballota lanata, which is cultivated in gardens, and Ballota suavelens or odoriferous ballots, which is recommended as an emmenagogue and antihysteric.

Black borehound is traditionally said to possess tonic, stomachic, antispasmodic, calming, depurative, diuretic, anthelmintic, resolvent and detersive properties.

The present invention is based on the discovery that extracts of black horehound originating from the whole plant, and especially from the aerial parts and in particular the stems and leaves, have valuable biological properties which can be used in the fields of cosmetics and pharmaceutics. The inventors have observed in particular that these extracts unexpectedly possess a melanogenesis-stimulating activity on the melanocytes present in the skin or the hair follicles, especially those on the scalp, and thus make it possible to promote the pigmentation of the skin or hair and to treat pigmentation disorders of the skin and hair by promoting more particularly the biosynthesis of melanin. Very good results in this field have been obtained with extracts of the whole plant, and especially of the aerial parts and in particular the stems and leaves of black horehound.

The inventors have also observed that the abovementioned extracts of black borehound are unexpectedly active in reducing the amount of triglycerides in the adipocytes, especially by inhibiting their synthesis in these cells. These extracts thus make it possible to prevent the development of accumulations of fat in the organism, such as cellulitis, so they are particularly useful for the preparation of cosmetic or pharmaceutical slimming compositions, especially dermatological slimming compositions.

One object of the present invention is therefore to solve the new technical problem which consists in providing a novel cosmetic or pharmaceutical composition, especially dermatological composition, intended in particular for promoting the pigmentation of the skin and for preventing or slowing down the appearance of white hair.

A further object of the present invention is to solve the new technical problem which consists in preparing a novel formulation of a cosmetic or pharmaceutical composition which has a good melanogenesis-stimulating activity on the melanocytes present in the skin or the hair follicles, especially those on the scalp.

A further object of the present invention is to provide a solution to the new technical problem which consists in providing a particularly easily obtainable plant extract which in itself has a good melanogenesis-stimulating activity on the melanocytes present in the skin or the hair follicles, without it being necessary to isolate an active substance of any kind, these isolation processes generally being lengthy and expensive.

A further object of the present invention is to solve the new technical problem which consists in preparing a novel formulation of a cosmetic or pharmaceutical composition which is active in reducing the amount of triglycerides in the adipocytes, thereby making it possible to prevent the development of accumulations of fat in the organism, such as cellulitis.

A further object of the present invention is to provide a solution to the new technical problem which consists in providing a particularly easily obtainable plant extract which in itself is active in reducing the amount of triglycerides in the adipocytes, without it being necessary to isolate an active substance of any kind, these isolation processes generally being lengthy and expensive.

All these new technical problems are solved for the first time by the present invention in a satisfactory manner which can be used on the industrial scale.

Thus, according to a first feature, the present invention relates to a cosmetic or pharmaceutical composition, especially dermatological composition, intended in particular for promoting the pigmentation of the skin, for preventing or slowing down the appearance of white hair, for reducing the amount of triglycerides in the adipocytes and for preventing the development of the accumulation of fat in the organism, such as cellulitis, said composition comprising as the active ingredient a cosmetically or pharmaceutically effective amount of an extract of black horehound, optionally in a cosmetically or pharmaceutically acceptable excipient.

In the present description and the claims, "cosmetically or pharmaceutically effective amount" is understood as meaning an amount at least equal to the minimum amount which is necessary for observing a significant cosmetic or pharmaceutical effect.

The extract of black horehound is advantageously selected from extracts of Ballota nigra, Ballota lanata and Ballota suavelens.

According to one particular characteristic of the invention, the extract of black horehound is selected from an extract of the whole plant and an extract of the aerial parts, and essentially the stems and leaves in particular.

According to another characteristic, the abovementioned extract of black horehound is an extract which is advantageously obtained by a process comprising at least one extraction step with, for example, a solvent selected from the group consisting of water, alcohols preferably containing from 1 to 4 carbon atoms, such as methanol, ethanol or propanol, a mixture of these alcohols with water, chlorinated solvents containing 1 or 2 carbon atoms, such as chloroform or dichloromethane, and organic esters preferably containing 3 to 6 carbon atoms, such as ethyl acetate. More generally, solvents which can also be used are organic solvents such as aromatic hydrocarbons, especially benzene, toluene or xylene, halogenated aliphatic or aromatic hydrocarbons, dialkyl ethers, dialkyl ketones, alkanols, carboxylic acids and their esters, or other solvents such as dimethylformamide, dioxane, tetrahydrofuran and dimethyl sulfoxide, or else super-critical carbon dioxide gas. The ratio of plant material to extraction agent can be chosen within a wide range, but is generally between 1:5 and 1:20 parts by weight and preferably about 1:10. The extraction is carried out at temperatures between room temperature and the boiling point of the solvent used for the extraction. A valuable extraction technique is the so-called Soxhlet extraction technique.

It is also possible, however, simply to carry out the extraction under reflux at normal atmospheric pressure for 2 to 4 h after the plant material has optionally been allowed to macerate in the cold for 2 to 4 h in the extraction solvent.

When extraction is complete, the phase containing the extract is filtered and then concentrated and/or evaporated to dryness under reduced pressure or by lyophilization.

This gives an extract according to the invention.

In general, the concentration of the extracts used according to the present invention for the preparation of a cosmetic or pharmaceutical composition, expressed by dry weight, is between 0.0001% and 5% by weight, preferably between 0.01% and 0.5% by weight, based on the total weight of the composition.

The cosmetic or pharmaceutical compositions, especially dermatological compositions, according to the present invention can be prepared in forms appropriate for a variety of modes of administration. In particular, they can be presented in a form intended for topical administration to the skin or scalp, such as a cream, a gel, a milk or a lotion, for promoting the pigmentation of the skin and preventing or slowing down the appearance of white hair.

Thus the cosmetic or pharmaceutical compositions, especially dermatological compositions, according to the invention have various applications in cosmetology or pharmacy, especially in dermatology, in particular when it is desired to restore normal pigmentation or increase this pigmentation.

For example, these compositions can be used as sun products for accelerating or intensifying tanning, which, in addition to the esthetic advantage often sought after, makes it possible to strengthen the natural defenses against ultraviolet radiation by increasing the melanin content of the epidermis. These compositions can also be used in the form of creams, for example, to give the skin a more sunburnt appearance, or else in the form of lotions for preventing or slowing down the appearance of white hair. Furthermore, in dermatology, the compositions according to the present invention can be used as therapeutic agents, either by themselves or in association with other drugs, in particular by topical administration in the treatment of melanocyte dysfunctions.

As far as the action on the melanocytes is concerned, it has been possible to demonstrate that the extracts according to the invention make it possible to favor the differentiation of the melanocytes, i.e. to favor the production of more mature or better differentiated melanosomes in human melanocyte cultures.

One particularly valuable application involves applying these extracts according to the invention in a method of treating melanocytes in culture, especially normal human melanocytes in culture, so as to cause them to acquire maturation properties appropriate for their subsequent use.

In particular, the subsequent use can consist of melanocyte grafts in humans, especially for treating certain pigmentation disorders such as vitiligo.

Furthermore, the cosmetic or pharmaceutical compositions, especially dermatological compositions, according to the invention also have various applications in cosmetology or pharmacy, especially in dermatology and particularly by topical administration, for reducing the amount of triglycerides in the adipocytes. It is known in particular that the synthesis of triglycerides by the adipocytes goes hand in hand with the development of accumulations of fat in the organism, such as cellulitis. Thus the extracts according to the invention have a particularly valuable application in cosmetic or pharmaceutical slimming compositions, especially dermatological slimming compositions, for preventing or treating excesses of fat, in particular cellulitis.

Advantageously, the abovementioned slimming compositions also contain other active substances such as xanthines, in particular caffeine, an extract of ivy (Hedera Hellix) or an extract of Coleus, in particular Coleus forskolii.

Advantageously, the cosmetic or pharmaceutical compositions according to the invention which are intended for topical administration are advantageously formulated with a particular excipient acting as a penetration vector, i.e. an agent which promotes penetration and diffusion in the skin structures in question, such as those commonly used in the fields of cosmetology and dermopharmacy, examples being ethyl alcohol, a glycol, in particular glycerol or propylene glycol, oleic acid, laurocapram or an essential oil, especially menthol or eucalyptol.

In one advantageous embodiment, a cosmetic or pharmaceutical composition according to the invention which is intended more particularly for the pigmentation of the skin or hair also contains a xanthine, in particular 1-methylxanthine, 3-methylxanthine, 3-isobutylmethylxanthine or theophylline, preferably at a concentration by weight of between 0.001% and 2% and particularly preferably of between 0.01% and 0.5%, based on the total weight of the composition.

In another embodiment, applicable in particular in the context of activating the pigmentation of the skin or hair, a cosmetic or pharmaceutical composition according to the invention also contains tyrosine or a derivative thereof such as glucose tyrosinate or N-malyltyrosine, preferably at a concentration by weight of between 0.001% and 10%, based on the total weight of the composition.

In yet another embodiment, applicable in particular in the context of activating the pigmentation of the hair, a cosmetic or pharmaceutical composition according to the invention also contains an effective concentration of at least one other active substance selected from vitamins, in particular the B vitamins, quinine or derivatives thereof, rubefacients such as methyl nicotinate, a papilla fibroblast culture supernatant as defined in the document EP-A-272 920, keratin hydrolyzates, trace elements such as zinc, selenium and copper, 5-α-reductase inhibitors such as progesterone, cyproterone acetate, minoxidil, azelaic acid and derivatives thereof, a 1,4-methyl-4-azasteroid, in particular 17-β-N,N-diethylcarbamoyl-4-methyl-4-aza-5-α-androstan-3-one, or else an extract of Serenoa repens.

In yet another embodiment, a cosmetic or pharmaceutical composition according to the invention also contains hydrated lipidic lamellar phases or liposomes, which may or may not incorporate the extract of Ballota nigra defined above.

According to a second feature, the present invention further relates to a process for the manufacture of a cosmetic or pharmaceutical composition, especially dermatological composition, intended in particular for promoting the pigmentation of the skin, for preventing or slowing down the appearance of white hair, for treating pigmentation disorders of the skin or hair, for reducing the amount of triglycerides in the adipocytes and for preventing the development of accumulations of fat in the organism, such as cellulitis, said process comprising the incorporation of at least one extract of black horehound, as defined above, into a cosmetically or pharmaceutically acceptable excipient, vehicle or carrier.

According to a third feature, the invention relates to the use of an extract of black horehound, as defined above, for the preparation of a cosmetic or pharmaceutical composition, especially dermatological composition, intended in particular for promoting the pigmentation of the skin, for preventing or slowing down the appearance of white hair, for treating pigmentation disorders of the skin or hair, for reducing the amount of triglycerides in the adipocytes and for preventing the development of accumulations of fat in the organism, such as cellulitis.

According to yet another feature, the present invention further relates to a cosmetic or therapeutic method of treating a pigmentation insufficiency or pigmentation disorders, said method comprising the application of an effective amount of at least one extract of black horehound, as defined above, advantageously incorporated in a cosmetically or pharmaceutically acceptable excipient, vehicle or carrier, preferably to the affected areas of the skin or scalp of a human being, so as to restore normal pigmentation of the skin or hair and/or increase this pigmentation.

According to yet another feature, the present invention further relates to a method of treating melanocytes in culture, especially human melanocytes in culture, so as to cause them to acquire maturation properties appropriate for subsequent use, said method comprising the cultivation of said melanocytes in a culture medium comprising an effective amount of at least one extract of black horehound for a sufficient period of time to obtain differentiation of the melanocytes.

According to yet another feature, the present invention relates to a cosmetic or therapeutic method of treatment consisting of melanocyte grafts in a mammal, preferably in man, said method comprising the grafting of melanocytes, especially human melanocytes, which have undergone differentiation by culture in the presence of an amount, effective for differentiation, of at least one extract of black horehound, as defined above.

According to yet another feature, the present invention relates to a cosmetic or therapeutic method of treatment for reducing the amount of triglycerides in the adipocytes of a mammal, in particular a human being, said method comprising the application to the areas to be treated, in a preventive or curative capacity, of an amount, effective for reducing the amount of triglycerides in the adipocytes, in particular for inhibiting their synthesis by these cells, of at least one extract of black horehound, as defined above, optionally in a cosmetically or pharmaceutically acceptable excipient, vehicle or carrier.

The invention also covers a method of preventing or treating excesses of fat, in particular cellulitis, said method comprising the application to the areas of the body of a mammal, in particular a human being, suffering from excesses of fat in the organism, such as cellulitis, of an amount, effective for reducing said excesses of fat, of at least one extract of black horehound, as defined above, optionally in a cosmetically or pharmaceutically acceptable excipient, vehicle or carrier.

In all the foregoing features, the extract of black horehound, as defined above, can be used in the presence of hydrated lipidic lamellar phases or liposomes, which may or may not incorporate said extract. It is pointed out that the expression "incorporate" covers the case where the extract is totally incorporated and the case or only a certain amount of this extract is incorporated in the hydrated lipidic lamellar phases or in the liposomes.

The term "lipidic" in the expression "lipidic lamellar phase" covers all substances which comprise a so-called fatty hydrocarbon chain generally containing more than 5 carbon atoms, this substance usually being called a "lipid".

According to the invention, the lipids used to form the lipidic lamellar phases or the liposomes are amphiphilic lipids, i.e. lipids consisting of molecular which possess either an ionic or a non-ionic hydrophilic group and a lipophilic group, these amphiphilic lipids being capable of forming lipidic lamellar phases or liposomes in the presence of an aqueous phase, depending on the amount of water in the mixture.

The following may be mentioned in particular among these lipids: phospholipids, phosphoaminolipids, glycolipids, polyoxyethylenated fatty alcohols and optionally polyoxyethylenated polyol esters. Such substances consist for example of an egg or soya lecithin, a phosphatidylserine, a sphyngomyelin, a cerebroside or an oxyethylenated polyglycerol stearate.

It is preferable according to the invention to use a mixture of lipids consisting of at least one amphiphilic lipid and at least one hydrophobic lipid such as a sterol like cholesterol or β-sitosterol. The amount of hydrophobic lipid, expressed in mol, must not generally exceed the amount of amphiphilic lipid and preferably must not be more than 0.5 times this amount.

The compounds or the extracts containing these compounds used according to the present invention can be incorporated into hydrated lipidic lamellar phases or into liposomes by known preparative techniques described for example in the document EP-B1-0 087 993=U.S. Pat. No. 4,508,703, if appropriate in combination with the document EP-B1-0 107 559=U.S. Pat. No. 4,621,023.

Other objects, characteristics and advantages of the invention will become clearly apparent from the following explanatory description referring to several Examples, which are given simply by way of illustration.

In fact, the present invention is in no way limited to the embodiments which have been described and illustrated. Thus, for example, it also covers a cosmetic or dermatological composition intended for preventing or slowing down the graying of the eyebrows or eyelashes.

The percentages are given by weight in the Examples, unless indicated otherwise.

EXAMPLE 1

Preparation of a methanolic extract of black horehound

500 g of aerial parts of Ballota nigra, made up essentially of stems and leaves, are treated under reflux for 3 h with about 5 l of methanol.

The methanolic extracts are filtered and the filtrate is evaporated under reduced pressure and then lyophilized to give a methanolic extract of Ballota nigra called extract I₁.

EXAMPLE 2

Preparation of an ethyl acetate extract of black horehound

The procedure described in Example 1 is followed, except that the solvent used is ethyl acetate; this gives an ethyl acetate extract of Ballota nigra called extract I₂.

EXAMPLE 3

Incorporation of an extract of whole black horehound plants into hydrated lipidic lamellar phases or into liposomes

An extract of whole Ballota nigra plants called extract I₃, obtained by following the procedure described in Example 1, except that the whole plants are used, is incorporated into hydrated lipidic lamellar phases or into liposomes by the preparative technique below:

The following are weighed out:

soya lecithin: 1.8 g

β-sitosterol: 0.2 g

lyophilized extract I₃ of Ballota nigra: 0.03 g

These constituents are dissolved in a mixture consisting of 25 ml of dichloromethane and 10 ml of methanol.

The resulting mixture is evaporated on a rotary evaporator at a temperature of 60° C. under reduced pressure.

The resulting lipidic film is then taken up and dispersed in distilled water qsp 50 g at room temperature for 12 h, with agitation.

The suspension of lipidic vesicles obtained is then homogenized by treatment with ultrasound for 10 min. at 4° C. at a power of 150 W.

The liposomes obtained in this way have a mean size of about 140 nm.

In one advantageous variant, this suspension is then gelled by being mixed with 50 g of 1.25% Carbopol® 940 gel, separately prepared in conventional manner. This gives about 100 g of a gelled suspension of liposomes at least partially encapsulating the extract of black horehound, the concentration of which is about 0.030%, based on the total weight of the suspension.

This gel is called "composition I₄ " and can be used as such within the framework of the invention.

EXAMPLE 4

Measurement of the efficacy of extracts of black borehound according to the invention on melanocytes in culture

Protocol:

S91 murine melanocytes, inoculated at a rate of 10⁵ cells per dish, are cultivated in EMEM complemented with non-essential amino acids and also containing 1% of fetal calf serum and 0.08 μg/ml of mitomycin C. 24 h after inoculation, the culture medium is replaced with fresh medium containing no mitomycin C and only comprising complemented EMEM, 1% of fetal calf serum and, where appropriate, the test product solubilized in DMSO at a concentration of about 40 mg/ml.

Six days after inoculation, the cells are removed and isolated by centrifugation and the cellular residue is recovered and dissolved in 0.5N sodium hydroxide solution in a sufficient proportion to obtain essentially the same concentration by weight of cells per milliliter of final solution.

The optical density of the solution obtained is read on a spectrophotometer at 405 nm, making it possible to evaluate the amount of melanin formed by comparison with the optical density of a solution of melanin of known concentration.

The cells are also counted and the amount of melanin formed per 10⁶ cells is calculated.

Extracts I₁ and I₂ of Ballota nigra were tested at various concentrations in micrograms (μg) per milliliter, as also mentioned in Tables I and II below.

In a separate experiment, an equivalent test was carried out to check that the melanocytes used in the present assays gave a positive response to beta-MSH (Melanocyte-Stimulating Hormone).

The melanogenesis-stimulating efficacy E of the test products is calculated by means of the following formula: ##EQU1## in which the quantities q represent the amounts of melanin formed per 10⁶ cells:

q_(p) : culture receiving the test product

q_(o) : control culture receiving no product.

The efficacy E of the extracts tested at different concentrations, calculated by means of the above formula, with:

a) extract I₁ of Example 1, or

b) with extract I₂ of Example 2,

is shown respectively in Tables I and II below.

The assays were performed with three dishes per concentration and per product, so the values shown in Tables I and II relating to the number of cells per dish and the amount of melanins, expressed in micrograms (μg) (per 10⁶ cells), are mean values.

A statistical study by the Student t test compares the results of the control cultures with those of the cultures treated with the products according to the invention.

S=significant at 5%,

NS=not significant at 5%.

                                      TABLE I                                      __________________________________________________________________________     Test with extract I, of Ballota nigra (aerial parts)                                   Number of                                                              Concentration                                                                          cells ± standard                                                                     Melanin, μg                                                of extract                                                                             deviation per                                                                           per 10.sup.6                                                                          Efficacy                                                                            Significance                                      I.sub.1 (μg/ml)                                                                     dish × 10.sup.-3                                                                  cells  E (%)                                                                               t                                                 __________________________________________________________________________      0 (control)                                                                           82 ± 8                                                                               55 ± 4                                                                                0 --                                                 2.5    81 ± 2                                                                               57 ± 4                                                                              +3  NS                                                 10     76 ± 4                                                                               62 ± 3                                                                             +12  NS                                                 25     77 ± 4                                                                               66 ± 6                                                                             +20  S                                                 100     75 ± 7                                                                               71 ± 5                                                                             +29  S                                                 __________________________________________________________________________

                                      TABLE II                                     __________________________________________________________________________     Test with extract I.sub.2 of Ballota nigra (aerial parts)                              Number of                                                              Concentration                                                                          cells ± standard                                                                     Melanin, μg                                                of extract                                                                             deviation per                                                                           per 10.sup.6                                                                          Efficacy                                                                            Significance                                      I.sub.2 (μg/ml)                                                                     dish × 10.sup.-3                                                                  cells  E (%)                                                                               t                                                 __________________________________________________________________________      0 (control)                                                                           80 ± 6                                                                               53 ± 4                                                                               0  --                                                 2.5     70 ± 11                                                                             62 ± 2                                                                             +16  S                                                 10      67 ± 5                                                                               72 ± 3                                                                             +35  S                                                 25      70 ± 7                                                                                73 ± 11                                                                           +37  S                                                 __________________________________________________________________________

Tables I and II above show that, at non-cytotoxic doses, the extracts according to the invention stimulate the production of melanin to a significant extent, representing a totally unexpected result for those skilled in the art.

In a separate experiment, it was also demonstrated that the extracts of black horehound according to the invention favor the differentiation of the melanocytes by the formation, within the melanocytes, of a larger number of mature melanosomes transferable to the keratinocytes.

EXAMPLE 5

Demonstration of the activity of the products of the invention on the differentiation of melanocytes in culture

The process of pigmentation of the skin's epidermis is known to involve differentiation of the melanocytes situated in the basal layer of the epidermis. This differentiation generally comprises four different stages (I to IV) corresponding to the accumulation of the pigment, i.e. the melanin, within the melanosomes (cellular organelles for storing and transferring the melanin). Stage IV (the most strongly colored) is the final stage of the charging of the melanosomes with pigment, so these melanosomes are considered to be mature. It is also known that it is at this stage that the melanin contained in the melanosomes is transferred to the keratinocytes situated at a higher level in the epidermis, via the dendritic extensions of the melanocytes.

Description of the assay:

Normal human melanocytes, isolated in conventional manner in the course of a face-lift on a 50-year-old woman, are placed on day D=0 in complete M 199 culture medium (GIBCO) comprising 10% v/v of fetal calf serum and supplemented with conventional growth factors.

On day D=3, 10 μg/ml of extract 12 of black horehound (ethyl acetate extract) of Example 2, solubilized in-DMSO, are added to the culture medium.

On day D=6, the medium is renewed with a medium of identical composition which also contains 10 μg/ml of extract I₂.

On day D=9, the cells are included in EPON 812® resin (glycerol diglycidyl and triglycidyl ether) available from LADD, Vermont, USA. The blocks of resin are then cut into ultrafine sections by means of a microtome. The ultrastructure of the cells can thus be observed by transmission electron microscopy.

In a parallel procedure, a control culture of melanocytes was prepared from the same source and under the same conditions, except that no extract was added to the culture from day D=3, only DMSO being added at the same concentration, i.e. 0.1% by volume.

Observation by electron microscopy shows that the control culture exhibits mainly stage I and II melanosomes. Furthermore, in the melanocytes, the reticuloendothelial system and the Golgi apparatus display little activity.

By contrast, the treated culture exhibits numerous melanosomes which have reached stages III and IV in the majority of cells. The reticuloendothelial system and the Golgi apparatus of the cells, which is where tyrosinase synthesis and glycosylation and the formation of the melanin-secreting vesicles take place, are very developed and hence very active. These characteristics together indicate the existence of differentiated melanocytes, especially insofar as they possess numerous stage III and IV mature melanosomes.

Thus the demonstration of a mechanism of action of the extracts of black horehound makes it possible on the one hand to explain the activity of the compositions according to the invention which promote the pigmentation of the skin, and on the other hand to carry out a process for the cultivation of more highly differentiated melanocytes with melanosomes of greater maturity, it then being possible for these melanocytes to be used in grafts for treating certain pigmentation disorders such as vitiligo.

EXAMPLE 6

Demonstration of the inhibitory activity of the products or the invention on the accumulation of triglycerides in the adipocytes

Triglycerides, which constitute an important energy reserve of the organism, are formed from glycerol and fatty acids in the intestinal wall, the liver and the adipose tissues.

Excesses of fat in the organism are thus associated directly with the accumulation of-triglycerides in the adipocytes.

Furthermore, it is known that certain lines of fibroblasts in culture, in particular the 3T3-L1 line, are capable of differentiating into adipocytes when the culture conditions allow (for example according to the technique described by Teruo Kawada et al. in Comp. Biochem. Physiol. (1990) vol. 96A, N.2, pp. 323-326).

Thus, to demonstrate the inhibitory activity of the products of the invention on the accumulation of triglycerides in the adipocytes, a culture of this line was prepared under conditions which permitted their differentiation into adipocytes, in the presence of ¹⁴ C-labeled glucose and in the presence or absence of a product according to the invention.

The glycerol utilized by the cells to synthesize the triglycerides originates indirectly from the glycolysis of glucose. Thus, under the conditions of the test performed, it will suffice to measure the radioactivity of the triglycerides extracted at the end of the experiment in order to assess the accumulation of triglycerides by the adipocytes.

On day D=0, Petri dishes of diameter 35 mm, containing 2 ml of a culture medium consisting of complete EMEM containing 10% v/v of fetal calf serum, are inoculated with 2×10⁵ cells/dish of the 3T3-L1 line (available from ATCC, reference CCL 92-1).

On day D=1, the culture medium is replaced with that used on day D=0 to which the differentiating agents, namely 100 μg/ml of isobutylmethylxanthine (IBMX) and 0.1 μg/ml of dexamethasone, mitomycin C and ¹⁴ C-glucose at a concentration of 0.5 μCi/ml have been added. This culture medium also contains the test products, with the exception of the medium corresponding to the control cultures.

On day D=7, the triglycerides present in the cultures are extracted with heptane. This is done by first removing the cells in culture from their dish in conventional manner by means of a trypsin solution. The resulting cell suspension is then lyzed by the addition of a sufficient amount of Dole's reagent (Dole V.P. et al., Journal of Biological Chemistry (1960) vol. 235, N.9, pp. 2595). Water and then heptane are subsequently added to the preparation to give two phases, the one aqueous and the other organic and consisting of heptane. The heptane phase, containing the triglycerides present in the culture, is then collected and its radioactivity is determined by liquid scintillation, for example by means of an apparatus of the KONTRON BETA V® type.

The measurement of the radioactivity of the extracts obtained from the cultures containing the product of the invention, compared with the measurement of the control cultures, therefore makes it possible to evaluate the inhibition of the accumulation of triglycerides, the latter being formed from the radioactive glucose not extracted by the heptane.

Thus the activity A of the products of the invention is calculated by means of the following formula: ##EQU2## R_(t) being the radioactivity of the triglyceride extracts of the control cultures, expressed in cpm (counts per minute), and

R_(p) being the radioactivity of the cultures in the presence of the product according to the invention, also expressed in cpm.

The product of the invention forming the subject of the present assay consists of methanolic extract I₁ of black horehound obtained according to

EXAMPLE 1

Table III below shows the results of the inhibitory activity of extract I₁ at two different concentration values in the cultures.

                  TABLE III                                                        ______________________________________                                         I.sub.1  Radioactivity R                                                                              Activity Significance                                   (μg/ml)                                                                              (cpm)         A        t                                              ______________________________________                                         50       14,199 ± 409                                                                              44.2%    S                                              10       20,434 ± 907                                                                              19.8%    S                                              Control  25,463 ± 1,890                                                                            0                                                       ______________________________________                                    

The significance of the results was calculated by the Student t test with p<0.05.

This Table clearly shows that the presence of extract I₁ according to the invention substantially and significantly inhibits the accumulation Of triglycerides in adipocytes in culture.

The products of the invention can thus advantageously be used as the active principle in cosmetic or pharmaceutical compositions, especially dermatological compositions, for preventing or treating excesses of fat, in particular cellulitis.

Various Formulation Examples of cosmetic or pharmaceutical compositions, especially dermatological compositions, are now given below.

EXAMPLE 7

    ______________________________________                                         Lotion for promoting the pigmentation of the hair:                             ______________________________________                                         extract I.sub.2 (Example 1)                                                                             0.15 g                                                propylene glycol         5 g                                                   Cremophor RH40 ®     1 g                                                   ethanol                  30 g                                                  perfumed aqueous excipient qsp                                                                          100 g                                                 ______________________________________                                    

The lotion is applied to the hair at a rate of 1 ml twice a day for 6 months to give a significant pigmentation effect.

EXAMPLE 8

Gel for promoting tanning

The gel is prepared from the following two phases A and B:

    ______________________________________                                         1) Phase A                                                                     extract I.sub.2 (Example 2)                                                                             0.1 g                                                 malyltyrosine            2 g                                                   propylene glycol         4 g                                                   glycerol                 0.5 g                                                 Cremophor RH40 ®     1 g                                                   ethanol                  25 g                                                  perfumed aqueous excipient qsp                                                                          50 g                                                  2) Phase B                                                                     1.25% Carbopol 940 ® gel                                                                            50 g                                                  ______________________________________                                    

Phase A is added gradually to phase B and the two are mixed with a propeller stirrer until dispersion is complete.

This gives a gel for promoting tanning of the skin, which can be applied before or during exposure to the sun.

EXAMPLE 9

    ______________________________________                                         Slimming composition                                                           ______________________________________                                         extract of black horehound according to                                                                   0.1 g                                               the invention (Example 1)                                                      96% alcohol                32 g                                                Carbopol 941 ®         2.5 g                                               aqueous excipient with preservative qsp                                                                   100 g                                               ______________________________________                                    

The extract of black horehound is first dissolved in the alcohol, after which the whole is incorporated into a gelled excipient containing the Carbopol.

This gives a slimming composition which can be applied to the areas to be treated. 

What is claimed is:
 1. A method for treating accumulations of fat, comprising applying to areas of the body of a person suffering from accumulations of fat, of an effective amount for reducing said accumulations of fat of at least one extract of black horehound.
 2. The method of claim 1, wherein said accumulations of fat are cellulitis.
 3. The method of claim 1, wherein said black horehound is selected from the group consisting of Ballota nigra, Ballota lanata and Ballota suavelens.
 4. The method of claim 1, wherein said extract of black horehound is an extract obtained by at least one extraction step with a solvent selected from the group consisting of water, an alcohol containing from 1 to 4 carbon atoms, a water/alcohol admixture, a chlorinated solvent from 1 to 2 carbon atoms, and an organic ester from 3 to 6 carbon atoms.
 5. The method of claim 4, wherein said alcohol is selected from the group consisting of methanol, ethanol and propanol.
 6. The method of claim 4, wherein said chlorinated solvent is selected from the group consisting of chloroform and dichloromethane.
 7. The method of claim 4, wherein said organic ester is ethyl acetate.
 8. The method of claim 1, wherein said method comprises applying said extract of black horehound at a concentration, expressed by dry weight, ranging between 0.0001% and 5% by weight, based on the total weight of the composition.
 9. The method of claim 1, wherein said extract of black horehound is applied at a concentration, expressed by dry weight, ranging between 0.01% and 0.5% by weight, based on the total weight of the composition.
 10. The method of claim 1, wherein said extract of black horehound is present in a composition comprising hydrated lipidic lamellar phases on liposomes.
 11. The method of claim 1, wherein said applying is by topical administration.
 12. A method for reducing accumulations of fat, comprising applying to areas of the body of a person of an effective amount for reducing the development of accumulations of fat in said person of at least one extract of black horehound.
 13. The method of claim 12, wherein said applying is by topical administration.
 14. The method of claim 12, wherein black horehound is selected from the group consisting of Ballota nigra, Ballota lanata and Ballota suavelens.
 15. The method of claim 12, wherein said extract of black horehound is an extract obtained by at least one extraction step with an organic solvent selected from the group consisting of an alcohol containing from 1 to 4 carbon atoms, a water/alcohol admixture, a chlorinated solvent from 1 to 2 carbon atoms, and an organic ester from 3 to 6 carbon atoms.
 16. The method of claim 15, wherein said alcohol is selected from the group consisting of methanol, ethanol and propanol.
 17. The method of claim 15, wherein said chlorinated solvent is selected from the group consisting of chloroform and dichloromethane.
 18. The method of claim 15, wherein said organic ester is ethyl acetate.
 19. The method of claim 12, wherein said method comprises applying said extract of black horehound at a concentration, expressed by dry weight, ranging between 0.0001% and 5% by weight, based on the total weight of composition.
 20. The method of claim 14, wherein said extract of black horehound is applied at a concentration, expressed by dry weight, ranging between 0.01% and 0.5% by weight, based on the total weight of the composition.
 21. The method of claim 14, wherein said extract of black horehound is present in a composition comprising hydrated lipidic lamellar phases on liposomes. 